DE69117840T2 - Polyacetalresin-Zusammensetzung mit Steifigkeit bei hoher Temperatur - Google Patents
Polyacetalresin-Zusammensetzung mit Steifigkeit bei hoher TemperaturInfo
- Publication number
- DE69117840T2 DE69117840T2 DE69117840T DE69117840T DE69117840T2 DE 69117840 T2 DE69117840 T2 DE 69117840T2 DE 69117840 T DE69117840 T DE 69117840T DE 69117840 T DE69117840 T DE 69117840T DE 69117840 T2 DE69117840 T2 DE 69117840T2
- Authority
- DE
- Germany
- Prior art keywords
- group
- carbon atoms
- polyacetal resin
- chain
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 229920006324 polyoxymethylene Polymers 0.000 title claims description 71
- 229930182556 Polyacetal Natural products 0.000 title claims description 68
- 239000011342 resin composition Substances 0.000 title claims description 38
- 229920005989 resin Polymers 0.000 claims description 64
- 239000011347 resin Substances 0.000 claims description 64
- 125000004432 carbon atom Chemical group C* 0.000 claims description 54
- 229920006122 polyamide resin Polymers 0.000 claims description 46
- 239000000203 mixture Substances 0.000 claims description 34
- 239000000945 filler Substances 0.000 claims description 31
- 125000000217 alkyl group Chemical group 0.000 claims description 30
- 150000001875 compounds Chemical class 0.000 claims description 25
- 239000002270 dispersing agent Substances 0.000 claims description 23
- 238000002844 melting Methods 0.000 claims description 23
- 230000008018 melting Effects 0.000 claims description 23
- 239000003365 glass fiber Substances 0.000 claims description 19
- 239000002245 particle Substances 0.000 claims description 19
- 125000003118 aryl group Chemical group 0.000 claims description 18
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 18
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 18
- -1 carbodiimide compound Chemical class 0.000 claims description 12
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 claims description 10
- 239000005057 Hexamethylene diisocyanate Substances 0.000 claims description 10
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 10
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims description 10
- 229920001577 copolymer Polymers 0.000 claims description 9
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 claims description 7
- 229920000299 Nylon 12 Polymers 0.000 claims description 7
- 230000005540 biological transmission Effects 0.000 claims description 6
- 229920001778 nylon Polymers 0.000 claims description 6
- MTZUIIAIAKMWLI-UHFFFAOYSA-N 1,2-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC=C1N=C=O MTZUIIAIAKMWLI-UHFFFAOYSA-N 0.000 claims description 5
- 239000005058 Isophorone diisocyanate Substances 0.000 claims description 5
- KXBFLNPZHXDQLV-UHFFFAOYSA-N [cyclohexyl(diisocyanato)methyl]cyclohexane Chemical compound C1CCCCC1C(N=C=O)(N=C=O)C1CCCCC1 KXBFLNPZHXDQLV-UHFFFAOYSA-N 0.000 claims description 5
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims description 5
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 claims description 4
- 239000004677 Nylon Substances 0.000 claims description 4
- 229920002292 Nylon 6 Polymers 0.000 claims description 4
- 229920000305 Nylon 6,10 Polymers 0.000 claims description 4
- 230000001476 alcoholic effect Effects 0.000 claims description 4
- 125000000524 functional group Chemical group 0.000 claims description 4
- 150000002357 guanidines Chemical class 0.000 claims description 4
- 229940083094 guanine derivative acting on arteriolar smooth muscle Drugs 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 239000011159 matrix material Substances 0.000 claims description 4
- 150000007974 melamines Chemical class 0.000 claims description 4
- 150000003672 ureas Chemical class 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 3
- 125000004849 alkoxymethyl group Chemical group 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 239000012948 isocyanate Substances 0.000 claims description 3
- 229920000049 Carbon (fiber) Polymers 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 229920000571 Nylon 11 Polymers 0.000 claims description 2
- 125000005907 alkyl ester group Chemical group 0.000 claims description 2
- 239000004917 carbon fiber Substances 0.000 claims description 2
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 claims description 2
- 239000000835 fiber Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 150000002513 isocyanates Chemical class 0.000 claims description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 2
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 229920000572 Nylon 6/12 Polymers 0.000 claims 1
- 150000008064 anhydrides Chemical group 0.000 claims 1
- 238000004898 kneading Methods 0.000 description 17
- 125000005704 oxymethylene group Chemical group [H]C([H])([*:2])O[*:1] 0.000 description 10
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 9
- 238000012360 testing method Methods 0.000 description 9
- 238000005299 abrasion Methods 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 7
- 239000000956 alloy Substances 0.000 description 5
- 229910045601 alloy Inorganic materials 0.000 description 5
- 125000005702 oxyalkylene group Chemical group 0.000 description 5
- 229920005992 thermoplastic resin Polymers 0.000 description 5
- BNCADMBVWNPPIZ-UHFFFAOYSA-N 2-n,2-n,4-n,4-n,6-n,6-n-hexakis(methoxymethyl)-1,3,5-triazine-2,4,6-triamine Chemical compound COCN(COC)C1=NC(N(COC)COC)=NC(N(COC)COC)=N1 BNCADMBVWNPPIZ-UHFFFAOYSA-N 0.000 description 4
- 239000004952 Polyamide Substances 0.000 description 4
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 4
- 125000002510 isobutoxy group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])O* 0.000 description 4
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 4
- 238000001000 micrograph Methods 0.000 description 4
- 125000006606 n-butoxy group Chemical group 0.000 description 4
- 125000003506 n-propoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 4
- 125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 4
- 229920002647 polyamide Polymers 0.000 description 4
- 125000005920 sec-butoxy group Chemical group 0.000 description 4
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 4
- 239000000454 talc Substances 0.000 description 4
- 229910052623 talc Inorganic materials 0.000 description 4
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
- 229930040373 Paraformaldehyde Natural products 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 238000005452 bending Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 229920001519 homopolymer Polymers 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 230000003014 reinforcing effect Effects 0.000 description 3
- UYVWNPAMKCDKRB-UHFFFAOYSA-N 1,2,4,5-tetraoxane Chemical compound C1OOCOO1 UYVWNPAMKCDKRB-UHFFFAOYSA-N 0.000 description 2
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 2
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 229920002302 Nylon 6,6 Polymers 0.000 description 2
- 229920002614 Polyether block amide Polymers 0.000 description 2
- 229920012196 Polyoxymethylene Copolymer Polymers 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- 238000003917 TEM image Methods 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 239000007822 coupling agent Substances 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 238000004870 electrical engineering Methods 0.000 description 2
- 239000012760 heat stabilizer Substances 0.000 description 2
- 238000011089 mechanical engineering Methods 0.000 description 2
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- VFKBNRYIYZIRMD-UHFFFAOYSA-N methyl n-(methoxymethyl)carbamate Chemical compound COCNC(=O)OC VFKBNRYIYZIRMD-UHFFFAOYSA-N 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 125000006353 oxyethylene group Chemical group 0.000 description 2
- 238000005453 pelletization Methods 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- 239000012756 surface treatment agent Substances 0.000 description 2
- 239000013638 trimer Substances 0.000 description 2
- IVHGQRJQXVQZIL-UHFFFAOYSA-N 1,1,3-tris(methoxymethyl)urea Chemical compound COCNC(=O)N(COC)COC IVHGQRJQXVQZIL-UHFFFAOYSA-N 0.000 description 1
- TWPQPSSERVQRKB-UHFFFAOYSA-N 1,1-bis(methoxymethyl)-3,3-dimethylurea Chemical compound COCN(COC)C(=O)N(C)C TWPQPSSERVQRKB-UHFFFAOYSA-N 0.000 description 1
- HTQXIHCFJIPGPV-UHFFFAOYSA-N 1,1-bis(methoxymethyl)urea Chemical compound COCN(C(N)=O)COC HTQXIHCFJIPGPV-UHFFFAOYSA-N 0.000 description 1
- FQERLIOIVXPZKH-UHFFFAOYSA-N 1,2,4-trioxane Chemical compound C1COOCO1 FQERLIOIVXPZKH-UHFFFAOYSA-N 0.000 description 1
- AUAGGMPIKOZAJZ-UHFFFAOYSA-N 1,3,6-trioxocane Chemical compound C1COCOCCO1 AUAGGMPIKOZAJZ-UHFFFAOYSA-N 0.000 description 1
- XKALZGSIEJZJCZ-UHFFFAOYSA-N 1,3-bis(methoxymethyl)urea Chemical compound COCNC(=O)NCOC XKALZGSIEJZJCZ-UHFFFAOYSA-N 0.000 description 1
- PZYIPPIXNPEYSH-UHFFFAOYSA-N 1-(methoxymethyl)-3-methylurea Chemical compound CNC(=O)NCOC PZYIPPIXNPEYSH-UHFFFAOYSA-N 0.000 description 1
- QHSJQEMESPRTBF-UHFFFAOYSA-N 2-(dimethoxymethyl)guanidine Chemical compound COC(OC)N=C(N)N QHSJQEMESPRTBF-UHFFFAOYSA-N 0.000 description 1
- BOLVKBXIEFIFQF-UHFFFAOYSA-N 2-(methoxymethyl)guanidine Chemical compound COCN=C(N)N BOLVKBXIEFIFQF-UHFFFAOYSA-N 0.000 description 1
- DOVPKQYCDOFPFT-UHFFFAOYSA-N 2-(trimethoxymethyl)guanidine Chemical compound COC(OC)(OC)N=C(N)N DOVPKQYCDOFPFT-UHFFFAOYSA-N 0.000 description 1
- DLTLLZLEJKRETK-UHFFFAOYSA-N 2-n,2-n,4-n,4-n,6-n-pentamethoxy-6-n-methyl-1,3,5-triazine-2,4,6-triamine Chemical compound CON(C)C1=NC(N(OC)OC)=NC(N(OC)OC)=N1 DLTLLZLEJKRETK-UHFFFAOYSA-N 0.000 description 1
- UQYWYFJGLYMBCC-UHFFFAOYSA-N 2-n-(dimethoxymethyl)-1,3,5-triazine-2,4,6-triamine Chemical compound COC(OC)NC1=NC(N)=NC(N)=N1 UQYWYFJGLYMBCC-UHFFFAOYSA-N 0.000 description 1
- KFVIYKFKUYBKTP-UHFFFAOYSA-N 2-n-(methoxymethyl)-1,3,5-triazine-2,4,6-triamine Chemical compound COCNC1=NC(N)=NC(N)=N1 KFVIYKFKUYBKTP-UHFFFAOYSA-N 0.000 description 1
- AOSPVUKRNAQARI-UHFFFAOYSA-N 2-n-(trimethoxymethyl)-1,3,5-triazine-2,4,6-triamine Chemical compound COC(OC)(OC)NC1=NC(N)=NC(N)=N1 AOSPVUKRNAQARI-UHFFFAOYSA-N 0.000 description 1
- HVZSUNIUNNGCMQ-UHFFFAOYSA-N 3-ethyl-1,1-bis(methoxymethyl)urea Chemical compound CCNC(=O)N(COC)COC HVZSUNIUNNGCMQ-UHFFFAOYSA-N 0.000 description 1
- 239000005046 Chlorosilane Substances 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 229920003189 Nylon 4,6 Polymers 0.000 description 1
- 229920009382 Polyoxymethylene Homopolymer Polymers 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000006230 acetylene black Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- NLEPDOASNNDPBD-UHFFFAOYSA-N bis(methoxymethyl)carbamic acid Chemical compound COCN(C(O)=O)COC NLEPDOASNNDPBD-UHFFFAOYSA-N 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 150000001718 carbodiimides Chemical class 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical compound Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- ZHCJJZJPLRFHMH-UHFFFAOYSA-N ethyl n-(methoxymethyl)carbamate Chemical compound CCOC(=O)NCOC ZHCJJZJPLRFHMH-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 125000000457 gamma-lactone group Chemical group 0.000 description 1
- 230000014509 gene expression Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical group O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- XKKFHYIHXAEDLW-UHFFFAOYSA-N methoxymethylcarbamic acid Chemical compound COCNC(O)=O XKKFHYIHXAEDLW-UHFFFAOYSA-N 0.000 description 1
- HJYNGRZUBXMFGB-UHFFFAOYSA-N methoxymethylurea Chemical compound COCNC(N)=O HJYNGRZUBXMFGB-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000009719 polyimide resin Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000013519 translation Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L59/00—Compositions of polyacetals; Compositions of derivatives of polyacetals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
- C08G18/4054—Mixtures of compounds of group C08G18/60 with other macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/205—Compounds containing groups, e.g. carbamates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/29—Compounds containing one or more carbon-to-nitrogen double bonds
- C08K5/31—Guanidine; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L59/00—Compositions of polyacetals; Compositions of derivatives of polyacetals
- C08L59/02—Polyacetals containing polyoxymethylene sequences only
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/20—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP21714990 | 1990-08-20 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE69117840D1 DE69117840D1 (de) | 1996-04-18 |
| DE69117840T2 true DE69117840T2 (de) | 1996-11-07 |
Family
ID=16699628
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE69117840T Expired - Fee Related DE69117840T2 (de) | 1990-08-20 | 1991-08-19 | Polyacetalresin-Zusammensetzung mit Steifigkeit bei hoher Temperatur |
Country Status (9)
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5298537A (en) * | 1992-04-09 | 1994-03-29 | E. I. Du Pont De Nemours And Company | Polyoxymethylene compositions containing at least one encapsulated nucleant |
| BR9305567A (pt) * | 1992-06-30 | 1994-12-27 | Polyplastics Co | Composição de poli-oxi-metileno |
| AU669567B2 (en) * | 1992-10-30 | 1996-06-13 | Basf Corporation | Water dispersible ionic and nonionic polyamide modified polyurethane resins for use in coating compositions |
| JP3285480B2 (ja) * | 1995-09-29 | 2002-05-27 | ポリプラスチックス株式会社 | ポリアセタール樹脂組成物 |
| US5902517A (en) * | 1996-10-28 | 1999-05-11 | Cabot Corporation | Conductive polyacetal composition |
| CN1276952C (zh) * | 2001-12-21 | 2006-09-27 | 三菱瓦斯化学株式会社 | 热塑性树脂组合物 |
| US7256966B2 (en) * | 2001-12-25 | 2007-08-14 | Asahi Kasei Chemicals Corporation | Ramp made of polyoxymethylene resin |
| US6974849B2 (en) * | 2003-03-03 | 2005-12-13 | Ticona Llc | Polyacetals with improved resistance to bleach |
| EP2084221A2 (en) * | 2006-11-22 | 2009-08-05 | E.I. Du Pont De Nemours And Company | Static dissipative polyacetal compositions |
| WO2014126626A1 (en) | 2013-02-15 | 2014-08-21 | Empire Technology Development Llc | Phenolic epoxy compounds |
| CN105408411B (zh) | 2013-06-13 | 2018-04-06 | 英派尔科技开发有限公司 | 多官能酚醛树脂 |
| EP3077364A4 (en) | 2013-12-02 | 2017-11-08 | Empire Technology Development LLC | Novel gemini surfactants and their use |
| WO2015084299A1 (en) * | 2013-12-02 | 2015-06-11 | Empire Technology Development Llc | Gemini surfactants and methods for their preparation and use |
| US9896637B2 (en) | 2015-04-08 | 2018-02-20 | Jtekt Corporation | Sliding member, method of manufacturing sliding member, and gear |
| JP2017061638A (ja) * | 2015-09-25 | 2017-03-30 | 富士ゼロックス株式会社 | 樹脂組成物、樹脂成形体、及び樹脂組成物の製造方法 |
| WO2017064778A1 (ja) * | 2015-10-14 | 2017-04-20 | Ykk株式会社 | ポリアセタール樹脂組成物、ファスニング部材及びスライドファスナー |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE626284A (enrdf_load_stackoverflow) * | 1962-04-28 | |||
| US3549734A (en) * | 1967-06-27 | 1970-12-22 | Takeshi Yasuda | Method of forming microfibers |
| GB1455314A (en) * | 1973-01-30 | 1976-11-10 | Asahi Chemical Ind | Resin composition |
| JPS5915948B2 (ja) * | 1974-12-16 | 1984-04-12 | 旭化成株式会社 | ポリアミド組成物 |
| JPS5381562A (en) * | 1976-12-24 | 1978-07-19 | Toyobo Co Ltd | Flame-retardant polyamide composition |
| JPS59105047A (ja) * | 1982-12-07 | 1984-06-18 | Mitsubishi Gas Chem Co Inc | アセタ−ル樹脂組成物 |
| DE3248330A1 (de) * | 1982-12-28 | 1984-06-28 | Bayer Ag, 5090 Leverkusen | Brandwidrig ausgeruestete polyamidformmassen |
| CA1235246A (en) * | 1984-10-25 | 1988-04-12 | Kavilipalayam M. Natarajan | Oxymethylene polymer molding compositions having enhanced resistance to speck formation |
| KR880005196A (ko) * | 1986-10-23 | 1988-06-28 | 로버어트 에이 롱맨 | 안정화된 옥시메틸렌 중합체 조성물 |
| CN1011040B (zh) * | 1986-11-18 | 1991-01-02 | 赫希斯特人造丝公司 | 颜色稳定度得到改善的聚缩醛稳定剂组合物 |
| US4873282A (en) * | 1987-05-15 | 1989-10-10 | Mitsubishi Petrochemical Co., Ltd. | Polyacetal resin composition |
| GB2210048B (en) * | 1987-09-22 | 1992-04-15 | Asahi Chemical Ind | Polyacetal composition |
| KR920005338B1 (ko) * | 1988-08-12 | 1992-07-02 | 가부시기가이샤 도시바 | 전자기기용 가동기구재료 |
| DE3834547A1 (de) * | 1988-10-11 | 1990-04-19 | Basf Ag | Polyoxymethylen-formmassen mit verbesserter thermischer stabilitaet, verfahren zu deren herstellung und deren verwendung |
| KR920702702A (ko) * | 1989-06-15 | 1992-10-06 | 미리엄 디이 메코너헤이 | 안정화 폴리아세탈 조성물 |
| KR0146285B1 (ko) * | 1989-08-09 | 1998-08-17 | 마에다 가쓰노스께 | 폴리옥시메틸렌 다원공중합체 및 그의 성형품 |
| JPH06334377A (ja) * | 1993-05-19 | 1994-12-02 | Toshiba Chem Corp | 電子機器筐体 |
-
1991
- 1991-08-09 TW TW080106300A patent/TW200514B/zh active
- 1991-08-13 FR FR9110275A patent/FR2665904B1/fr not_active Expired - Fee Related
- 1991-08-15 JP JP03228520A patent/JP3109753B2/ja not_active Expired - Fee Related
- 1991-08-16 US US07/746,341 patent/US5354798A/en not_active Expired - Fee Related
- 1991-08-19 DE DE69117840T patent/DE69117840T2/de not_active Expired - Fee Related
- 1991-08-19 GB GB9117870A patent/GB2247684B/en not_active Expired - Fee Related
- 1991-08-19 BE BE9100752A patent/BE1004773B3/fr not_active IP Right Cessation
- 1991-08-19 EP EP91113855A patent/EP0475127B1/en not_active Expired - Lifetime
- 1991-08-20 KR KR1019910014355A patent/KR950006140B1/ko not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JP3109753B2 (ja) | 2000-11-20 |
| KR950006140B1 (ko) | 1995-06-09 |
| GB9117870D0 (en) | 1991-10-09 |
| TW200514B (enrdf_load_stackoverflow) | 1993-02-21 |
| EP0475127A1 (en) | 1992-03-18 |
| BE1004773B3 (fr) | 1994-11-03 |
| FR2665904A1 (fr) | 1992-02-21 |
| GB2247684A (en) | 1992-03-11 |
| KR920004498A (ko) | 1992-03-27 |
| EP0475127B1 (en) | 1996-03-13 |
| US5354798A (en) | 1994-10-11 |
| FR2665904B1 (fr) | 1993-12-31 |
| DE69117840D1 (de) | 1996-04-18 |
| BE1004773A0 (fr) | 1993-01-26 |
| JPH05239313A (ja) | 1993-09-17 |
| GB2247684B (en) | 1993-10-06 |
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